JP2008204777A - Active material for lithium battery and its manufacturing method, and lithium battery using the active material - Google Patents
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本発明は、安価で毒性の少ない、高性能(高容量)な酸化鉄超微粒子からなるリチウム電池用活物質、およびその製造方法、並びに該活物質を用いたリチウム電池に関するものである。 The present invention relates to an active material for a lithium battery comprising high-performance (high capacity) iron oxide ultrafine particles that is inexpensive and less toxic, a method for producing the same, and a lithium battery using the active material.
現在我が国においては、携帯電話、ノートパソコンなどの携帯型電子機器に搭載されている二次電池のほとんどは、リチウム二次電池である。また、リチウム二次電池は、今後ハイブリッドカー、電力負荷平準化システムなどの大型電池としても実用化されるものと予測されており、その重要性はますます高まっている。 Currently, in Japan, most of the secondary batteries installed in portable electronic devices such as mobile phones and notebook computers are lithium secondary batteries. In addition, lithium secondary batteries are expected to be put into practical use as large batteries such as hybrid cars and power load leveling systems in the future, and their importance is increasing.
このリチウム二次電池は、いずれもリチウムを可逆的に吸蔵・放出することが可能な材料を含有する正極および負極、さらに非水系電解液を含むセパレータまたは固体電解質を主要構成要素とする。 This lithium secondary battery has a positive electrode and a negative electrode containing materials capable of reversibly occluding and releasing lithium, and a separator or a solid electrolyte containing a non-aqueous electrolyte as main components.
これらの構成要素のうち、電極用の活物質として検討されているのは、リチウムコバルト酸化物(LiCoO2)、リチウムマンガン酸化物(LiMn2O4)、リチウムチタン酸化物(Li4Ti5O12)などの酸化物系;金属リチウム、リチウム合金、スズ合金などの金属系;および黒鉛、MCMB(メソカーボンマイクロビーズ)などの炭素系材料が挙げられる。 Among these constituent elements, lithium cobalt oxide (LiCoO 2 ), lithium manganese oxide (LiMn 2 O 4 ), and lithium titanium oxide (Li 4 Ti 5 O) are considered as active materials for electrodes. 12 )); metal systems such as metallic lithium, lithium alloys and tin alloys; and carbon-based materials such as graphite and MCMB (mesocarbon microbeads).
これらの材料について、それぞれの活物質中のリチウム含有量における、化学ポテンシャルの差によって、電池の電圧が決定される。そして、電極を構成する材料の組み合わせによって、大きな電位差を形成できることが、エネルギー密度に優れるリチウム二次電池の特徴である。 For these materials, the battery voltage is determined by the difference in chemical potential in the lithium content of each active material. A feature of a lithium secondary battery having excellent energy density is that a large potential difference can be formed by a combination of materials constituting the electrode.
特に、リチウムコバルト酸化物LiCoO2活物質と炭素材料を電極とした組み合わせにおいて、4V近い電圧が可能となり、また充放電容量(電極から脱離・挿入可能なリチウム量)も大きいことから、この電極材料の組み合わせが、現行のリチウム二次電池において広く採用されている。 In particular, in the case of using a lithium cobalt oxide LiCoO 2 active material and a carbon material as an electrode, a voltage close to 4 V is possible, and the charge / discharge capacity (the amount of lithium that can be desorbed and inserted from the electrode) is large. A combination of materials is widely adopted in current lithium secondary batteries.
しかしながら、このLiCoO2は、稀少金属であるコバルトを主成分として含むために、リチウム二次電池の高コストの要因の一つとなっている。さらに、現在すでに全世界のコバルト生産量の約20%が電池産業において用いられていることを考慮すれば、LiCoO2からなる正極材料のみでは、今後の需要拡大に対応可能かどうかは、不明である。 However, since this LiCoO 2 contains cobalt, which is a rare metal, as a main component, it is one of the high cost factors of the lithium secondary battery. Furthermore, considering that about 20% of the world's cobalt production is already used in the battery industry, it is unclear whether only the cathode material made of LiCoO 2 can meet future demand growth. is there.
一方、コバルトよりもさらに安価なマンガン、チタンを用いたLiMn2O4活物質とLi4Ti5O12活物質を含む電極の組み合わせにより、リチウムの吸蔵・脱離反応がスムーズに行われやすく、また反応に伴う結晶格子体積の変化がより少ないことから、長期にわたる充放電サイクルに優れたリチウム二次電池が可能となることが明らかとなっており、一部は実用化されている。しかしながら、LiCoO2と比べて容量が小さいことが問題となっている。また、50℃以上におけるマンガンの電解液への溶解に起因する顕著な特性劣化という問題点も有しているので、この材料によるLiCoO2の代替は、予期された程には進展していない。 On the other hand, the combination of an electrode containing LiMn 2 O 4 active material and Li 4 Ti 5 O 12 active material using manganese and titanium, which is cheaper than cobalt, facilitates the lithium occlusion / desorption reaction smoothly. Further, since the change in the volume of the crystal lattice associated with the reaction is smaller, it has been clarified that a lithium secondary battery excellent in charge / discharge cycles over a long period of time becomes possible, and some of them have been put into practical use. However, there is a problem that the capacity is smaller than that of LiCoO 2 . Further, since there is a problem of remarkable characteristic deterioration due to dissolution of manganese in an electrolytic solution at 50 ° C. or higher, substitution of LiCoO 2 by this material has not progressed as expected.
今後、リチウム二次電池は、自動車用電源や大容量のバックアップ電源、緊急用電源など、大型で長寿命のものが必要となることが予測されることから、前項のような酸化物活物質に比べ、より安価で毒性の少ない、さらに高性能(高容量)な電極活物質が必要とされていた。 In the future, lithium secondary batteries are expected to require large-sized and long-life batteries such as automobile power supplies, large-capacity backup power supplies, and emergency power supplies. In comparison, there has been a need for a cheaper, less toxic, and higher performance (high capacity) electrode active material.
一方、酸化鉄は、LiCoO2、LiMn2O4、Li4Ti5O12等の酸化物活物質比べ、さらに安価で毒性の低い物質であることから、電極活物質としての利用が期待されていた。 On the other hand, iron oxide is expected to be used as an electrode active material because it is cheaper and less toxic than oxide active materials such as LiCoO 2 , LiMn 2 O 4 , and Li 4 Ti 5 O 12. It was.
一般的な粒子径の酸化鉄にはリチウムが挿入・脱離できず、リチウム電池活物質として機能しないとされていたが、近年、酸化鉄を微粒子化することにより、充放電可能であることが公知となった。 It has been said that lithium cannot be inserted into or extracted from iron oxide having a general particle size and does not function as a lithium battery active material. However, in recent years, it is possible to charge and discharge by making iron oxide fine particles. It became publicly known.
電池特性は、酸化鉄の粒子径と相関があり、より微細化するほど向上することが知られている。例えば、カットオフ電位1.0Vでの初期放電容量は、1μmの粒子径では、55mAh/gの容量が得られ、一次粒子径が7nmの凝集体では、230mAh/gの容量が得られている。(非特許文献1参照)
また、一次粒子径が20nmで比較的凝集が抑えられた酸化鉄微粒子を使用した場合には、電池の充放電サイクル特性は良好であるが、約80mAh/g程度の放電容量しか得られておらず、数十ナノメートルの粒子サイズでは電池特性が不十分であり、実用に適する電池は得られていなかった。(非特許文献2参照)
これまで、リチウム電池活物質として報告されてきた酸化鉄は、溶液中に前駆体を昇温度の遅い通常のヒーター加熱により析出させ、この前駆体を乾燥後、電気炉で焼成する合成法が主に採用されてきた。このため一次粒子径が微細であっても凝集体であり、また、粒子径も不均一であり、良好な電池特性は得られていなかった。 Until now, iron oxide, which has been reported as a lithium battery active material, is mainly synthesized by depositing a precursor in a solution by heating with a normal heater with a slow temperature rise, drying the precursor, and then firing it in an electric furnace. Has been adopted. For this reason, even if the primary particle size is fine, it is an aggregate, and the particle size is also nonuniform, and good battery characteristics have not been obtained.
一方、マイクロ波加熱は、均一且つ急速な加熱が可能であることから、均一な粒子径を有し、高い結晶性を有する微粒子を合成する方法として有望であることが知られている。これまで、鉄イオンを含む溶液にマイクロ波を照射し、酸化鉄微粒子を製造する方法が知られていた(非特許文献3参照)。しかしながらが、粒子サイズと昇温速度との相関関係の検討がなされておらず、単分散の一次粒子が得られるものの、粒子サイズは50〜100nm程度であった。そして、マイクロ波加熱で合成された酸化鉄微粒子の電池特性についての報告例は、これまで存在しない。
したがって、本発明者等は実用化可能なリチウム電池用の活物質を得るには、数ナノメートル程度のサイズを有し、且つ数十ナノメートルの粗大粒子を含まない程度に粒子径の分布幅が小さく、電池特性に優れる酸化鉄超微粒子を、低コストで効率良く製造する技術が必要であると考えた。 Therefore, in order to obtain a practically usable active material for a lithium battery, the present inventors have a particle size distribution width that has a size of about several nanometers and does not include coarse particles of several tens of nanometers. Therefore, it was considered necessary to have a technique for efficiently producing iron oxide ultrafine particles having a small size and excellent battery characteristics at low cost.
本発明は、上記のような現状の課題を解決し、充放電容量が大きく、且つサイクル特性が良好な電極材料となる酸化鉄超微粒子からなるリチウム電池用活物質およびその低コストで効率的な製造方法、並びに該活物質を含む電極材料を用いた電池特性に優れたリチウム電池を提供することを目的とする。 The present invention solves the above-mentioned problems as described above, and is an active material for lithium batteries composed of ultrafine iron oxide particles that is an electrode material having a large charge / discharge capacity and good cycle characteristics, and its low-cost and efficient It is an object of the present invention to provide a lithium battery excellent in battery characteristics using a manufacturing method and an electrode material containing the active material.
本発明者等は鋭意検討した結果、1〜10nmの範囲の平均粒子径を有し、且つ粒子径の分布幅が1〜10nmである酸化鉄超微粒子が、リチウム電池用活物質として優れた性状を有すること、および鉄イオンを含む溶液にマイクロ波を照射することによって、前記酸化鉄超微粒子を簡単に製造できることを発見し、本発明を完成したものである。 As a result of intensive studies, the present inventors have found that iron oxide ultrafine particles having an average particle diameter in the range of 1 to 10 nm and a particle diameter distribution range of 1 to 10 nm are excellent properties as an active material for a lithium battery. And the present invention has been completed by discovering that the iron oxide ultrafine particles can be easily produced by irradiating a solution containing iron ions with microwaves.
すなわち、本発明は、次の1〜5の構成をとるものである
1.平均粒子径が1〜10nmの範囲で、且つ粒子径の分布幅が1〜10nmの範囲である酸化鉄超微粒子からなるリチウム電池用活物質。
2.鉄を含む化合物を溶媒中に溶解してなる溶液にマイクロ波を照射して1〜10分以内で80℃〜120℃に急速加熱を施すことを特徴とする1に記載のリチウム電池用活物質用の製造方法。
3.照射するマイクロ波の周波数が、300MHz〜3THzであることを特徴とする2に記載の製造方法。
4.液中の鉄イオンの濃度が0.01〜5Mであることを特徴とする2又は3に記載の製造方法。
5.正極および負極として使用する2つの電極と、電解質からなるリチウム電池において、電極を構成する材料として請求項1に記載のリチウム電池用活物質を用いたことを特徴とするリチウム電池。
That is, this invention takes the structure of the following 1-5. An active material for a lithium battery comprising iron oxide ultrafine particles having an average particle size in the range of 1 to 10 nm and a particle size distribution range of 1 to 10 nm.
2. 2. The active material for a lithium battery according to 1, wherein a solution obtained by dissolving a compound containing iron in a solvent is irradiated with microwaves and rapidly heated to 80 ° C. to 120 ° C. within 1 to 10 minutes. Manufacturing method.
3. 3. The manufacturing method according to 2, wherein the frequency of the irradiated microwave is 300 MHz to 3 THz.
4). 4. The production method according to 2 or 3, wherein the concentration of iron ions in the liquid is 0.01 to 5M.
5. A lithium battery comprising the two electrodes used as a positive electrode and a negative electrode and an electrolyte, wherein the lithium battery active material according to claim 1 is used as a material constituting the electrode.
本発明によれば、平均粒子径が1〜10nmの範囲で、且つ粒子径の分布幅が1〜10nmの範囲である酸化鉄超微粒子からなる、安価で毒性の少なく充放電特性に優れたリチウム電池用活物質を、低コストで効率良く製造することが可能となる。そして、この酸化鉄超微粒子活物質をリチウム電池用の電極材料として使用することにより、優れた特性を有するリチウム電池が得られる。 According to the present invention, lithium which is composed of iron oxide ultrafine particles having an average particle size in the range of 1 to 10 nm and a particle size distribution range of 1 to 10 nm, which is inexpensive, has low toxicity and has excellent charge / discharge characteristics. The battery active material can be efficiently produced at low cost. And the lithium battery which has the outstanding characteristic is obtained by using this iron oxide ultrafine particle active material as an electrode material for lithium batteries.
本発明のリチウム電池用活物質となる酸化鉄超微粒子は、平均粒子径が1〜10nmの範囲で、且つ粒子径の分布幅が1〜10nm、好ましくは1〜5nmの範囲であることを特徴とする。このリチウム電池活物質用酸化鉄超微粒子は、鉄を含む化合物を溶媒中に溶解してなる溶液にマイクロ波を照射して熱処理を施すことによって、製造することができる。 The iron oxide ultrafine particles used as the active material for a lithium battery of the present invention are characterized in that the average particle diameter is in the range of 1 to 10 nm and the distribution width of the particle diameter is in the range of 1 to 10 nm, preferably 1 to 5 nm. And The iron oxide ultrafine particles for a lithium battery active material can be produced by irradiating a solution obtained by dissolving a compound containing iron in a solvent with heat treatment.
そして、この酸化鉄超微粒子からなるリチウム電池用活物質を含有する電極を構成要素として用いたリチウム電池は、高容量で、かつ可逆的なリチウム挿入・脱離反応が可能であり、高い信頼性が期待できる電池である。このリチウム電池は、一次電池としても、また二次電池としても使用可能である。 A lithium battery using an electrode containing an active material for a lithium battery made of ultrafine iron oxide particles as a constituent element has a high capacity and a reversible lithium insertion / extraction reaction, and has high reliability. Can be expected. This lithium battery can be used as a primary battery or a secondary battery.
以下、本発明でリチウム電池用活物質として用いる酸化鉄超微粒子の製造方法について、詳細に説明する。
(リチウム電池用活物質の製造)
本発明において、リチウム電池用活物質として用いる酸化鉄超微粒子の製造に用いる原料は、鉄を含有する化合物であれば特に制限されず、例えばFe(NO3)3・9H2O、FeSO4・7H2O、FeCl3・6H2O等の金属塩が挙げられる。
Hereinafter, the manufacturing method of the iron oxide ultrafine particles used as the active material for the lithium battery in the present invention will be described in detail.
(Manufacture of active materials for lithium batteries)
In the present invention, the raw material used for producing the iron oxide ultrafine particles used as the active material for the lithium battery is not particularly limited as long as it is a compound containing iron. For example, Fe (NO 3 ) 3 · 9H 2 O, FeSO 4 · Examples thereof include metal salts such as 7H 2 O and FeCl 3 .6H 2 O.
はじめに、前記原料を溶媒中に溶解してなる溶液を調製する。溶媒の種類は、前記原料が溶解し、マイクロ波を吸収すれば特に制限されないが、好ましくは蒸留水が上げられる。溶液中の鉄の濃度は特に制限されないが、通常は0.01〜5M程度、好ましくは0.05〜1M程度、特に好ましくは0.1M程度とすればよい。 First, a solution prepared by dissolving the raw materials in a solvent is prepared. The type of the solvent is not particularly limited as long as the raw material dissolves and absorbs microwaves, but preferably distilled water is used. The concentration of iron in the solution is not particularly limited, but is usually about 0.01 to 5M, preferably about 0.05 to 1M, and particularly preferably about 0.1M.
つづいて、前記溶媒にマイクロ波を照射して熱処理を施す。マイクロ波の周波数は、300MHz〜3THz、好ましくは300MHz〜300GHzの範囲であれば特に制限されず、例えば市販の加熱装置に使用されている2.45GHzとすることができる。熱処理の温度は、70℃〜120℃、好ましくは80℃〜110℃、より好ましくは95℃〜105℃の範囲である。昇温速度は、マイクロ波照射開始から1分〜10分以内に、室温から80℃以上、好ましくは95℃以上、より好ましくは100℃以上までに加熱する。 Subsequently, heat treatment is performed by irradiating the solvent with microwaves. The frequency of the microwave is not particularly limited as long as it is in the range of 300 MHz to 3 THz, preferably 300 MHz to 300 GHz. For example, it can be 2.45 GHz used in a commercially available heating apparatus. The temperature of heat processing is 70 to 120 degreeC, Preferably it is 80 to 110 degreeC, More preferably, it is the range of 95 to 105 degreeC. The heating rate is from 1 minute to 10 minutes from the start of microwave irradiation and heating from room temperature to 80 ° C. or higher, preferably 95 ° C. or higher, more preferably 100 ° C. or higher.
なお、上記の熱処理条件の範囲をはずれた場合には、酸化物だけではなく水酸化物も同時に析出し、単相の試料として得られなくなる。 In addition, when the range of the above heat treatment conditions is deviated, not only oxides but also hydroxides are precipitated at the same time and cannot be obtained as a single-phase sample.
上記の熱処理によって溶液中に析出した酸化鉄超微粒子を乾燥するには、凝集を抑えた乾燥法であれば、特に限定されず、例えば凍結乾燥、噴霧乾燥等の公知の乾燥法を用いて乾燥することができる。 The drying of the iron oxide ultrafine particles precipitated in the solution by the heat treatment is not particularly limited as long as it is a drying method that suppresses aggregation. For example, drying is performed using a known drying method such as freeze drying or spray drying. can do.
(リチウム電池)
本発明のリチウム電池は、前記酸化鉄超微粒子活物質を含有する電極を構成部材として用いるものである。すなわち、電極材料のひとつに本発明の酸化鉄超微粒子活物質を用いる以外は、公知のリチウム電池(コイン型、ボタン型、円筒型、全固体型等)の電池要素をそのまま採用することができる。
図1は、本発明のリチウム電池を、コイン型電池に適用した1例を示す模式図である。このコイン型電池1は、負極端子2、負極3、(セパレータ+電解液)4、絶縁パッキング5、正極6、正極缶7により構成される。
(Lithium battery)
The lithium battery of the present invention uses an electrode containing the iron oxide ultrafine particle active material as a constituent member. That is, a battery element of a known lithium battery (coin type, button type, cylindrical type, all solid type, etc.) can be used as it is except that the iron oxide ultrafine particle active material of the present invention is used as one of electrode materials. .
FIG. 1 is a schematic view showing an example in which the lithium battery of the present invention is applied to a coin-type battery. The coin-type battery 1 includes a negative electrode terminal 2, a negative electrode 3, a (separator + electrolyte) 4, an insulating packing 5, a positive electrode 6, and a positive electrode can 7.
本発明では、上記本発明の酸化鉄超微粒子活物質に、必要に応じて導電剤、結着剤等を配合して電極合材を調製し、これを集電体に圧着することにより電極を作製する。集電体としては、好ましくはステンレスメッシュ、アルミ箔等を用いることができる。導電剤としては、好ましくはアセチレンブラック、ケッチェンブラック等を用いることができる。結着剤としては、好ましくはテトラフルオロエチレン、ポリフッ化ビニリデン等を用いることができる。 In the present invention, the iron oxide ultrafine particle active material of the present invention is mixed with a conductive agent, a binder or the like as necessary to prepare an electrode mixture, and this is crimped to a current collector to form an electrode. Make it. As the current collector, a stainless mesh, aluminum foil or the like can be preferably used. As the conductive agent, acetylene black, ketjen black or the like can be preferably used. As the binder, tetrafluoroethylene, polyvinylidene fluoride, or the like can be preferably used.
電極合材における酸化鉄超微粒子活物質、導電剤、結着剤等の配合割合は特に限定されないが、通常は導電剤が1〜30重量%程度、結着剤が0〜30重量%とし、残部を酸化鉄超微粒子活物質となるようにすれば良い。 The blending ratio of the iron oxide ultrafine particle active material, the conductive agent, the binder and the like in the electrode mixture is not particularly limited, but usually the conductive agent is about 1 to 30% by weight, the binder is 0 to 30% by weight, What is necessary is just to make it the remainder become an iron oxide ultrafine particle active material.
本発明のリチウム電池において、上記酸化鉄超微粒子を含有する電極に対する対極としては、例えば金属リチウム、リチウム合金など、負極として機能し、リチウムを吸蔵している公知のものを採用することができる。或いは、対極として、リチウムコバルト酸化物(LiCoO2)やスピネル型リチウムマンガン酸化物(LiMn2O4)などの、正極として機能し、かつリチウムを吸蔵している公知のものも採用することもできる。すなわち、組み合わせる電極構成材料によって、本発明の活物質を含有する電極は、正極としても、負極としても機能できる。 In the lithium battery of the present invention, a known electrode that functions as a negative electrode and occludes lithium, such as metal lithium and a lithium alloy, can be used as a counter electrode for the electrode containing the iron oxide ultrafine particles. Alternatively, as the counter electrode, a known one that functions as a positive electrode and occludes lithium, such as lithium cobalt oxide (LiCoO 2 ) or spinel type lithium manganese oxide (LiMn 2 O 4 ), can also be used. . That is, the electrode containing the active material of the present invention can function as a positive electrode or a negative electrode depending on the electrode constituent material to be combined.
また、本発明のリチウム電池において、セパレータ、電池容器等も公知の電池要素を採用すればよい。 In the lithium battery of the present invention, a known battery element may be adopted for the separator, the battery container, and the like.
さらに、電解質としても、公知の電解液、固体電解質等が適用できる。例えば、電解液としては、過塩素酸リチウム、6フッ化リン酸リチウム等の電解質を、エチレンカーボネート(EC)、ジメチルカーボネート(DMC)、プロピレンカーボネート(PC)、ジエチルカーボネート(DEC)等の溶媒に溶解させたものが使用できる。 Further, as the electrolyte, a known electrolytic solution, solid electrolyte, or the like can be applied. For example, as an electrolytic solution, an electrolyte such as lithium perchlorate or lithium hexafluorophosphate is used in a solvent such as ethylene carbonate (EC), dimethyl carbonate (DMC), propylene carbonate (PC), or diethyl carbonate (DEC). What was dissolved can be used.
つぎに、実施例により本発明の特徴とするところをより一層明確にするが、本発明は、これらの実施例に限定されるものではない。以下の例において、酸化鉄超微粒子の平均粒径および粒度分布は、日機装株式会社製、ナノトラック粒度分布測定装置(UPA150)を用い、動的光散乱法により測定した。粒子が数μm以下になると、溶媒分子運動の影響を受け、粒子がブラウン運動をする。この運動の速さは粒子の大きさによって異なり、これらの運動した粒子にレーザー光を照射すると、その速度に応じた位相の違う光の散乱が生じる。これを検出することにより粒度分布を求める方法が動的光散乱法である。 Next, the features of the present invention will be further clarified by examples, but the present invention is not limited to these examples. In the following examples, the average particle size and particle size distribution of the iron oxide ultrafine particles were measured by a dynamic light scattering method using a nanotrack particle size distribution measuring apparatus (UPA150) manufactured by Nikkiso Co., Ltd. When the particle is several μm or less, the particle is subjected to Brownian motion due to the influence of solvent molecular motion. The speed of this movement varies depending on the size of the particles, and when these moving particles are irradiated with laser light, light with different phases corresponding to the speed is scattered. A method of obtaining the particle size distribution by detecting this is the dynamic light scattering method.
[実施例1]
(リチウム電池用活物質の製造)
100mLの蒸留水にFe(NO3)3・9H2Oを加え、鉄の濃度が0.1Mの溶液を調製した。この溶液をガラス製のフラスコに移し、マイクロ波反応装置(四国計測工業株式会社製、簡易型マイクロ波反応装置)内に設置した。次いで、この溶液を攪拌しながら、2.45GHzのマイクロ波を2分間照射した。マイクロ波照射中に、温度は100℃に上昇し、溶液中へ超微粒子が析出した。
[Example 1]
(Manufacture of active materials for lithium batteries)
Of distilled water 100mL Fe (NO 3) 3 · 9H 2 O was added, the concentration of iron solution was prepared 0.1 M. This solution was transferred to a glass flask and installed in a microwave reactor (manufactured by Shikoku Keiki Kogyo Co., Ltd., simplified microwave reactor). Subsequently, 2.45 GHz microwave was irradiated for 2 minutes, stirring this solution. During microwave irradiation, the temperature rose to 100 ° C. and ultrafine particles were deposited in the solution.
上記熱処理によって溶液中へ析出した超微粒子の粒度分布を動的光散乱法により調べたところ、平均粒子径が7nmで、粒子径の分布幅が3nmであることが明らかとなった。(図2参照) When the particle size distribution of the ultrafine particles precipitated in the solution by the heat treatment was examined by a dynamic light scattering method, it was found that the average particle size was 7 nm and the particle size distribution width was 3 nm. (See Figure 2)
次に、上記溶液中へ析出した微粒子を凍結乾燥機により乾燥させ、酸化鉄超微粒子活物質を得た。得られた酸化鉄超微粒子の粒子形状を透過型電子顕微鏡により調べたところ、10nm以下の楕円形状を有する一次粒子から構成されていることが明らかとなった。(図3参照) Next, the fine particles precipitated in the solution were dried by a freeze dryer to obtain an iron oxide ultrafine particle active material. When the particle shape of the obtained iron oxide ultrafine particles was examined with a transmission electron microscope, it was revealed that the iron oxide ultrafine particles were composed of primary particles having an elliptical shape of 10 nm or less. (See Figure 3)
また、得られた酸化鉄超微粒子をX線粉末回折装置により調べたところ、公知のヘマタイト型の三酸化鉄(α−Fe2O3)であることが明らかとなった。(図4参照) Further, when the obtained iron oxide ultrafine particles were examined with an X-ray powder diffractometer, it was found to be known hematite type iron trioxide (α-Fe 2 O 3 ). (See Figure 4)
(リチウム電池)
このようにして得られた酸化鉄超微粒子活物質に、導電剤としてアセチレンブラック、結着剤としてポリフッ化ビニリデンを、重量比で4:2:1となるように配合して電極を作製した。そして、対極にリチウム金属を用いて、6フッ化リン酸リチウムをエチレンカーボネート(EC)とジエチルカーボネート(DEC)との混合溶媒(体積比1:1)に溶解させた1M溶液を電解液とする、図1に示す構造のリチウム電池(コイン型セル)を作製し、その電気化学的リチウム挿入・脱離挙動を測定した。電池の作製は、公知のセルの構成・組み立て方法に従って行った。
(Lithium battery)
The iron oxide ultrafine particle active material thus obtained was mixed with acetylene black as a conductive agent and polyvinylidene fluoride as a binder in a weight ratio of 4: 2: 1 to prepare an electrode. Then, using a lithium metal as a counter electrode, a 1M solution in which lithium hexafluorophosphate is dissolved in a mixed solvent (volume ratio 1: 1) of ethylene carbonate (EC) and diethyl carbonate (DEC) is used as an electrolytic solution. A lithium battery (coin-type cell) having the structure shown in FIG. 1 was prepared, and its electrochemical lithium insertion / extraction behavior was measured. The battery was produced according to a known cell configuration / assembly method.
作製されたリチウム電池について、25℃の温度条件下で、電流密度10mA/g、4.0V−1.0Vのカットオフ電位で電気化学的リチウム挿入・脱離試験を行ったところ、可逆的なリチウム挿入・脱離が可能であることが判明した。5サイクルまでの充放電特性を、図5に示す。初期放電容量は、405mAh/gであり、2サイクルから5サイクルの放電容量も約310mAh/gを維持しており、サイクル特性も良好であった。このことから、本発明の酸化鉄超微粒子活物質が、可逆性の高いリチウム挿入・脱離反応が可能であり、リチウム電池電極材料として有用であることが明らかとなった。 An electrochemical lithium insertion / extraction test was conducted on the fabricated lithium battery under a temperature condition of 25 ° C. with a current density of 10 mA / g and a cutoff potential of 4.0 V-1.0 V. It was found that lithium insertion / extraction was possible. The charge / discharge characteristics up to 5 cycles are shown in FIG. The initial discharge capacity was 405 mAh / g, the discharge capacity from 2 to 5 cycles also maintained about 310 mAh / g, and the cycle characteristics were also good. From this, it became clear that the iron oxide ultrafine particle active material of the present invention is capable of highly reversible lithium insertion / extraction reaction and is useful as a lithium battery electrode material.
本発明によれば、安価で毒性の低い鉄を主成分とした、安定に充放電可能なリチウム電池用活物質を得ることができる。また、その製造方法も、マイクロ波加熱により、常温・常圧付近の液相で迅速に合成可能な方法であることから、低コストで効率良く高付加価値の材料を製造することができる。 ADVANTAGE OF THE INVENTION According to this invention, the active material for lithium batteries which can charge / discharge stably can be obtained which has cheap and low toxicity iron as a main component. In addition, since the production method is also a method that can be rapidly synthesized in a liquid phase near room temperature and normal pressure by microwave heating, a high value-added material can be produced efficiently at low cost.
さらに、本発明の酸化鉄超微粒子活物質を電極材料として用いたリチウム電池は、可逆的なリチウム挿入・脱離反応が可能で、長期にわたる充放電サイクルに対応可能であり、また300mAh/g以上の高容量が期待できる電池である。 Furthermore, the lithium battery using the iron oxide ultrafine particle active material of the present invention as an electrode material is capable of reversible lithium insertion / extraction reaction, can be used for a long charge / discharge cycle, and is 300 mAh / g or more. It is a battery that can be expected to have a high capacity.
1 コイン型リチウム電池
2 負極端子
3 負極
4 セパレータ+電解液
5 絶縁パッキング
6 正極
7 正極缶
DESCRIPTION OF SYMBOLS 1 Coin type lithium battery 2 Negative electrode terminal 3 Negative electrode 4 Separator + Electrolyte 5 Insulation packing 6 Positive electrode 7 Positive electrode can
Claims (5)
A lithium battery comprising the two electrodes used as a positive electrode and a negative electrode and an electrolyte, wherein the lithium battery active material according to claim 1 is used as a material constituting the electrode.
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